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. 2024 Apr 30;19(4):e0298770. doi: 10.1371/journal.pone.0298770

Table 2. Factors associated with the therapeutic efficacy of atezolizumab plus bevacizumab in patients with unresectable hepatocellular carcinoma (HCC) assessed based on the best response on contrast-enhanced CT according to the modified response evaluation criteria in solid tumors (mRECIST) after 6 and 12 weeks of treatment.

a) Evaluation in a total of 67 patients                    
  Univariate analysis Multivariate analysis
Number of patients (%) p- Hazard ratio 95%CI p-
Total CR PR SD PD values values
Age: years < 70 22 1 (4.5) 07 (31.8) 12 (54.5) 02 (09.1) 0. 6675 1 0.319–3.420 0.9431
≥ 70 45 1 (2.2) 13 (28.9) 21 (46.7) 10 (22.2) 1.044
Etiology Viral 23 1 (4.3) 08 (34.8) 10 (43.5) 04 (17.4) 0. 4290 1 0.460–4.714 0.514
non-viral 44 1 (2.3) 12 (27.3) 23 (52.3) 08 (18.2) 1.473
mALBI 1/ 2a 42 1 (2.4) 12 (28.6) 21 (50.0) 08 (19.0) 0. 6707 1 0.191–2.089 0.4512
grades 2b 25 1 (4.0) 08 (32.0) 12(48.0) 04 (16.0) 0.631
BCLC A/ B 27 0 (0.0) 09 (33.3) 14 (51.9) 04 (14.8) 0. 9432 1 0.134–8.651 0.9456
Stages C 40 2 (5.0) 11 (27.5) 19 (47.5) 08 (20.0) 1.075
PVTT Absent 34 0 (0.0) 11 (32.4) 17 (50.0) 06 (17.6) 0. 9319 1 0.148–9.219 0.8833
Present 33 2 (6.1) 09 (27.3) 16 (48.5) 06 (18.2) 1.167
EH Absent 45 1 (2.2) 15 (33.3) 22 (48.9) 07 (15.6) 0. 4990 1 0.304–5.366 0.7383
Metastasis Present 22 1 (4.5) 05 (22.7) 11 (50.0) 05 (22.7) 1.277
AFP: ng/mL < 200 32 0 (0.0) 11 (34.4) 18 (56.3) 03 (09.4) 0. 7976 1 0.325–4.389 0.789
≥ 200 35 2 (5.7) 09 (25.7) 15 (42.9) 09 (25.7) 1.194
N/L ratio <2.7 32 0 (0.0) 11 (34.4) 13 (40.6) 08 (25.0) 0. 7976 1 0.320–3.068 0.9872
≥2.7 35 2 (5.7) 09 (25.7) 20 (57.1) 04 (11.4) 0.991
Previous TACE/TAI Absent 32 1 (3.1) 11 (34.4) 13 (40.6) 7 (21.9) 0.438 1 0.293–3.916 0.9176
Present 35 1 (2.9) 9 (25.7) 20 (57.1) 5 (14.3) 1.071
MTA Naïve 42 2 (4.8) 15 (35.7) 18 (42.9) 07 (16.7) 0. 0902 1 0.763–15.033 0.1087
Experienced 25 0 (0.0) 05 (20.0) 15 (60.0) 05 (20.0) 3.386
b) Evaluation in 65 patients consisting of 42 MTA-naïve patients and 23 patients after lenvatinib discontinuation due to PD or adverse events                    
  Univariate analysis Multivariate analysis
Number of patients (%) p- Hazard ratio 95%CI p-
Total CR PR SD PD values values
Age: years < 70 22 1 (4.5) 07 (31.8) 12 (54.5) 02 (09.1) 0.6174 1 0.273–3.233 0.9201
≥ 70 43 1 (2.3) 12 (27.9) 20 (46.5) 10 (23.3) 0.939
Etiology Viral 22 1 (4.5) 08 (36.4) 09 (40.9) 04 (18.2) 0.2914 1 0.508–5.702 0.3883
non-viral 43 1 (2.3) 11 (25.6) 23 (53.5) 08 (18.6) 1.702
mALBI 1/ 2a 41 1 (2.4) 11 (26.8) 21 (51.2) 08 (19.5) 0.4943 1 0.142–1.760 0.2801
grades 2b 24 1 (4.2) 08 (33.3) 11 (45.8) 04 (16.7) 0.499
BCLC A/ B 27 0 (0.0) 09 (33.3) 14 (51.9) 04 (14.8) 0.8815 1 0.220–22.011 0.502
Stages C 38 2 (5.3) 10 (26.3) 18 (47.4) 08 (21.1) 2.201
PVTT Absent 33 0 (0.0) 10 (30.3) 17 (51.5) 06 (18.2) 0.7257 1 0.073–6.288 0.7305
Present 32 2 (6.3) 09 (28.1) 15 (46.9) 06 (18.8) 0.676
EH Absent 45 1 (2.2) 15 (33.3) 22 (48.9) 07 (15.6) 0.4034 1 0.274–5.645 0.7774
Metastasis Present 20 1 (5.0) 04 (20.0) 10 (50.0) 05 (25.0) 1.244
AFP: ng/mL < 200 31 0 (0.0) 10 (32.3) 18 (58.1) 03 (09.7) 0.9935 1 0.316–4.485 0.7972
≥ 200 34 2 (5.9) 09 (26.5) 14 (41.2) 09 (26.5) 1.19
N/L ratio <2.7 31 0 (0.0) 10 (32.3) 13 (41.9) 08 (25.8) 0.9935 1 0.239–2.577 0.6889
≥2.7 34 2 (5.9) 09 (26.5) 19 (55.9) 04 (11.8) 0.784
Previous TACE/TAI Absent 32 1 (3.1) 11 (34.4) 13 (40.6) 7 (21.9) 0.3796 1 0.296–4.321 0.8563
Present 33 1 (3.9) 8 (24.2) 19 (57.6) 5 (15.2) 1.132
Lenvatinib Naïve 42 2 (4.8) 15 (35.7) 18 (42.9) 07 (16.7) 0.0642 1 0.924–25.409 0.0619
experienced 23 0 (0.0) 04 (17.4) 14 (60.9) 05 (21.7) 4.846